Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0410-2014 — Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used to inject PMMA cement into vertebral bodies during Vertebroplasty procedure.

U.S. FDA — Device Enforcement · United States · 2013-07-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0410-2014
Date of alert
2013-07-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Synthes USA HQ, Inc.
Product category
device
Product type
Devices
Reported risk: Complaints were received of inconsistencies in the expiration dates shown on the packaging of the Vertebroplasty Needle Kit 10g Diamond Tip device.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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